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Water was purified by a Millipore filtration system
The genetic causes of SCD include homozygosity for the rs334 mutation (HbSS, commonly referred as SCA) and compound heterozygosity between rs334 and mutations that lead to either other structural variants of -globin (such as HbC, causing HbSC) or reduced levels of -globin production as in -thalassemia (causing HbS/-thalassemia)
USING Fluorescent IN Situ Hybridization to Demonstrate Chromosomal Aberrations in Multiple Myeloma Patients Diploid by Conventional Cytogenetics
Impaired kidney function can also prevent you from efficiently converting vitamin D to its active form
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